Cyber Security Quality Engineer

Cyber security, Software development, Project management, Problem solving, Information security, Research and development, Customer experience, FDA, Pharmaceutics, Medical devices, Quality management, Communication skills, Documentation, Accountability, Product development, Implementation, QA, QMS, Team leadership, Software engineering, Mechanical engineering, Planning
Contract W2, Contract Independent, 12 Months
Depends on Experience
Travel not required

Job Description

Title: Cyber Security Quality Engineer

Location: Temecula, California

Duration: 12 Months+

USC & GC Preferred, the consultant must be on our W2

Consultant Must Have Pharmaceutical Client experience

Locals preferred

JOB DESCRIPTION:

Lead  Vascular cybersecurity quality engineering activities by developing and maintaining cybersecurity policy, standards, applications, systems, etc. Develop a risk-based cybersecurity program which meets regulatory requirements and aligns with industry leading information security practices. Work closely with R&D software engineers on threat identification and mitigation activities using industry leading cybersecurity controls and tools sets. Collaborate with business units, application development teams, and third-party vendors to achieve program requirements while enabling the business. Facilitate cross team coordination to achieve defined cybersecurity goals as well as meet technical requirements in support of detailed implementation plans for cybersecurity projects.

 

Job Duties:

  • Prepares overall project quality plans including milestones, validation processes and documentation procedures.
  • Conducts special analyses and projects as required.
  • Resolves and/or facilitates resolution of problems including identifying causes to prevent re-occurrence.
  • Responsible for problem resolution, communication and policy implementation.
  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), and other regulatory requirements.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
  • Performs other related duties and responsibilities, on occasion, as assigned.

 

Qualifications:

General Qualifications

  • A Bachelor's degree in an applicable engineering discipline with ten (10) plus years of progressively more responsible work experience in quality assurance and design related to medical devices, preferably in electro-mechanical and implantable medical devices (class III and IV).
  • Broad cross-disciplinary and in-depth knowledge and experience with industry accepted quality assurance design methodologies and project management tools.
  • Direct cybersecurity and product development experience.
  • Five years or more in quality or R&D engineering management.
  • Desired: An advanced credential in a relevant discipline/concentration. Professional certification or designation, such as CQE, CSQE, CRE and/or CMQ/OE.
  • Ability to work in a highly matrixed and geographically diverse business environment.
  • Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results.
  • Ability to work effectively within a team in a fast-paced changing environment.
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
  • Multi-tasks, prioritizes and meets deadlines in timely manner.
  • Strong organizational, planning, and follow-up skills and ability to hold others accountable.
  • Ability to maintain regular and predictable attendance.
Dice Id : 10450168
Position Id : DYESAL083112
Originally Posted : 2 weeks ago
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